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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849536Generated: November 2, 2026

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → HCID 86702881, compound

https://huagongshe.com/reaction/1849536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
Reactant3-Cyclohexyl-1-propanolHCID 70763—
Reactant5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
Reactant5-chloro-N-(N,N-dimethylsulfamoyl)-2,4-difluorobenzamideHCID 86702836—
ProductHCID 86702881HCID 86702881—

Reaction Steps

Following the procedure as described in Example 8 and making variations as required to replace 5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamide with 5-chloro-N—(N,N-dimethylsulfamoyl)-2,4-difluorobenzamide and adamantan-1-ylmethanol with 3-cyclohexylpropan-1-ol, the title compound was obtained as a colorless solid (0.03 g, 7%): 1H NMR (300 MHz, DMSO-d6) δ 11.75 (s, 1H), 7.72 (d, J=7.3 Hz, 1H), 7.23 (d, J=12.3 Hz, 1H), 4.12 (t, J=6.2 Hz, 2H), 2.87 (s, 6H), 1.80-1.58 (m, 7H), 1.35-1.11 (m, 6H), 0.94-0.88 (m, 2H); MS (ES−) m/z 419.2, 421.2 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-7c272ef4b338454abbacd74f0a149d2e
Source noteuspto-grants-2015_02